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PMA de la FDA

Stimulator, tibial, electrical, implantable, for urinary incontinence

Número de PMA: P200036 · 2026-09-09

SolicitanteBoston Scientific Corporation
Fecha de decisión2026-09-09
Número PMAP200036
Código de productoQPT
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorGU

Resumen del dispositivo

Stimulator, tibial, electrical, implantable, for urinary incontinence is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2026-09-09. The device is classified under product code QPT. It was reviewed by the GU advisory panel.

Preguntas frecuentes

What is the Stimulator, tibial, electrical, implantable, for urinary incontinence?

Stimulator, tibial, electrical, implantable, for urinary incontinence is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Boston Scientific Corporation.

When did Stimulator, tibial, electrical, implantable, for urinary incontinence receive FDA 510(k) clearance?

The clearance date for Stimulator, tibial, electrical, implantable, for urinary incontinence can be found in the official FDA records.

Who is the listed applicant for Stimulator, tibial, electrical, implantable, for urinary incontinence?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stimulator, tibial, electrical, implantable, for urinary incontinence?

The FDA product code for Stimulator, tibial, electrical, implantable, for urinary incontinence is QPT.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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